Canonical Allele Identifier: CA487267206

Gene: LTBP2

Linked Data

• gnomAD v4: 14-74503491-G-A
• MyVariant Identifiers: chr14:g.74970194G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503491G>A , CM000676.2:g.74503491G>A	GRCh38
NC_000014.8:g.74970194G>A , CM000676.1:g.74970194G>A	GRCh37
NC_000014.7:g.74039947G>A	NCBI36
NG_021486.1:g.113841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4698C>T MANE Select	ENSP00000261978.4:p.Cys1566=
ENST00000261978.8:c.4698C>T	ENSP00000261978.4:p.Cys1566=
ENST00000553939.5:c.4698C>T	ENSP00000452110.1:p.Cys1566=
ENST00000556690.5:c.4566C>T	ENSP00000451477.1:p.Cys1522=
NM_000428.2:c.4698C>T	NP_000419.1:p.Cys1566=
XM_011536765.1:c.4317C>T	XP_011535067.1:p.Cys1439=
XM_011536766.1:c.4239C>T	XP_011535068.1:p.Cys1413=
XM_011536767.1:c.4215C>T	XP_011535069.1:p.Cys1405=
XM_011536765.2:c.4317C>T	XP_011535067.1:p.Cys1439=
NM_000428.3:c.4698C>T MANE Select	NP_000419.1:p.Cys1566=